1. Controlling the epidemic_17Jul11 Controlling the epidemic Clinical considerations – design, set-up and conduct Sheena McCormack

2. Controlling the epidemic_17Jul11 A tale of two epidemics 1.Sub-Saharan Africa  Heterosexual women 2.UK  gay and other MSM  Starting with PrEP…

3. Controlling the epidemic_17Jul11 Concerns common to both Who will pay for it? Will people drift away from condom use?  Cannot be assessed in placebo controlled trials as placebo controls for behaviour Is there a danger of exploitation? How will PrEP be delivered [safely]?  Toxicity  Resistance

4. Controlling the epidemic_17Jul11 Safety  Generally very reassured by data in positive individuals and in trials to date  Serious adverse reactions only Resistance  Resistance more likely to come from treated population and reassured by DART in which viral load and resistance were not done in real time  Least concern with coital regimens which have limited systemic absorption Tenofovir gel, truvada tablets

5. Controlling the epidemic_17Jul11 0 20 40 60 80 100 LCM (n=590) CDM (n=617) LCM (n=109) CDM (n=78) <199200-9991000-9999≥10000 First-line ART Second-line ART N.B. 149 values of <400 c/ml imputed as <199 c/ml Percentage 0 20 40 60 80 100 LCM (n=590) CDM (n=617) LCM (n=109) CDM (n=78) <199200-9991000-9999≥10000 First-line ART Second-line ART N.B. 149 values of <400 c/ml imputed as <199 c/ml Percentage 0 20 40 60 80 100 LCM (n=590) CDM (n=617) LCM (n=109) CDM (n=78) <199200-9991000-9999≥10000 First-line ART Second-line ART N.B. 149 values of <400 c/ml imputed as <199 c/ml Percentage 0 20 40 60 80 100 LCM (n=590) CDM (n=617) LCM (n=109) CDM (n=78) <199200-9991000-9999≥10000 First-line ART Second-line ART N.B. 149 values of <400 c/ml imputed as <199 c/ml Percentage VL at 5y in DART, by monitoring strategy C Kityo, D Dunn, R Kasirye et al CROI 2011

6. Controlling the epidemic_17Jul11 Understand and build on successes in HIV prevention  Zambia ART coverage  Kenya MMC Forge partnerships between research, service and community Seek out champions in leadership positions Remember these are drugs, so we need clinicians, but we are not giving them to patients For delivery – know your service setting

7. Controlling the epidemic_17Jul11 Critical questions about efficacy of intermittent and coital regimens to answer  To improve acceptability by offering a choice that suits sexual lifestyle…which changes with time  Bonus being this will reduce the cost Need to demonstrate safe to reduce HIV, pregnancy and lab monitoring  Also to improve acceptability  Also bonus of reducing cost Back to design - feasibility

8. Controlling the epidemic_17Jul11 Epidemic 1 – heterosexual women Feasibility and cost-saving  We know women like using gel – multiple trials  Simplify dosing to a single dose pre-sex - simplifies training and social marketing, and halves cost  Reduce procedures especially HIV and pregnancy testing and stop routine laboratory monitoring  Demonstrate safe to continue in pregnancy  Demonstrate ease of transition to service providers

9. Controlling the epidemic_17Jul11 Epidemic 2 – gay/other MSM in UK Feasibility  Uptake and adherence – will anyone want it? Have to offer more than daily  Procedures need to mimic routine care  Concern regarding condom drift could be a barrier to funding – have behavioural and other interventions been given a proper chance?

10. Controlling the epidemic_17Jul11 Condom drift  Can only be assessed in an open-label design when participants know they are taking an effective alternative Exploitation  Also needs open-label design  Needs to be carefully solicited through qualitative research

11. CROI 16 th -19 th February 2010, San Francisco 11 Gel use at last sex act with/without Condom by Centre over Time

12. CROI 16 th -19 th February 2010, San Francisco 12 Condom use at last sex act with/without Gel by Centre over Time

13. Unprotected anal intercourse 1998 – 2008 UK gym surveys MSM %

14. Controlling the epidemic_17Jul11 Issues for the trials For how long will placebo be acceptable? Open label trials  Will participants share drug?  Negative result difficult to interpret without placebo controlled data for coital/intermittent regimens

15. Controlling the epidemic_17Jul11 A tale of two epidemics 1.Sub-Saharan Africa  Heterosexual women 2.UK  gay and other MSM  But it’s not just PrEP…

16. Controlling the epidemic_17Jul11 Clinical trial evidence for preventing sexual HIV transmission – 14 July 2011 Efficacy Study Effect size (CI) Medical male circumcision (Orange Farm, Rakai, Kisumu) 54% (38; 66) HIV Vaccine (Thailand) 31% (1; 51) 0% 10 20 30 40 50 60 70 80 90 100% 39% (6; 60) Tenofovir vaginal (SA) Truvada oral MSMs (America’s, Thailand, SA) 44% (15; 63) Treatment for prevention (Africa, Asia, America’s) 96% (73; 99) Truvada oral for heterosexuals (Botswana TDF2) 63% (21; 48) Tenofovir/truvada for discordant couples (Partners PrEP) 73% (49; 85) Truvada for women (Kenya, SA, Tanzania) 0% (-69; 41) Modified from Slim Karim 6 th Transmission Workshop, 2011

17. Controlling the epidemic_17Jul11 Epidemic 1 – heterosexual SSA Design  Incidence high enough to support cluster- randomised designs  Control clusters receive standard of care  Intervention clusters receive combination prevention – could have the toolkit and the garage  Incidence through structured x-sectional surveys Conduct  Clusters well defined and characterised  Communities engaged, government and ministry support essential  Large number of field staff needed

18. Controlling the epidemic_17Jul11 Concluding thoughts 1.Testing at the centre of all initiatives 2.The science has delivered, but successful implementation is all about behaviour 3.Know your epidemic, know your service setting, forge those partnerships and find the champions!

19. Controlling the epidemic_17Jul11 Acknowledgements  Slim for the trial evidence slide  MDP partners for prioritising questions and generating ideas for design and conduct in SSA for women  UK PrEP Working Group for prioritising and generating ideas for design and conduct in UK for MSM

20. Controlling the epidemic_17Jul11 Pregnancy rates & Outcomes among women on triple-drug antiretroviral therapy in the DART trial IAS 2009 60% tenofovir based regimen 206 live births and 26 stillbirths Any congenital abnormality reported7 (3.0%)  Congenital talipes (club foot)3 (2TDF, 1NVP)  Congenital hydrocephalus1 (died) (TDF)  Cardiac (PDA and ASD)1 (NVP)  Undescended testes1 (NVP)  Skin tag on neck1 (TDF) Rates similar to previously reported: 3.0/100 (2.4-3.7) HIV-infected women with first trimester ART in the Antiretroviral Pregnancy Register 2.7/100 live births in the CDC birth defects register 174/206 infants are enrolled into the separate infant follow up study. Of 137/174 (79%) for whom test results are available, none are HIV infected P Munderi; H Wilkes; D Tumukunde et al